ORGANOMETALLIC CHEMISTRY OF BINUCLEAR 1-A ZADIENE-NICKEL(0) COMPLEXES- BIMETALLIC COMPOUNDS WITH A NI-FE BOND BY ADDITION OF PENTACARBONYL-IRON(0) AND NICKELALACTONS BY RING-OPENING REACTION OF CYCLIC ANHYDRIDES
D. Walther et al., ORGANOMETALLIC CHEMISTRY OF BINUCLEAR 1-A ZADIENE-NICKEL(0) COMPLEXES- BIMETALLIC COMPOUNDS WITH A NI-FE BOND BY ADDITION OF PENTACARBONYL-IRON(0) AND NICKELALACTONS BY RING-OPENING REACTION OF CYCLIC ANHYDRIDES, Zeitschrift fur anorganische und allgemeine Chemie, 621(4), 1995, pp. 635-639
Citations number
9
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Zeitschrift fur anorganische und allgemeine Chemie
The binuclear nickel(0) complexes 1-3, which contain as well bridging
1-azadienes ligands as five or six-membered (NN)-chelate rings react a
t -30 degrees C with Fe(CO)(5) to form the bimetallic compounds 4-6, c
ontaining a Ni-Fe bond and two carbonyl groups as bridging ligands. Th
e coordination of the [(bpy)Ni(0)] fragment to the olefin part of the
1-azadiene chain in 6 leads to the formation of the trinuclear complex
7, which can storage CO, at the peripheral position. Succinic acid an
hydride or glutaric acid anhydrid undergo a ring opening reaction by r
eacting with 3 yield nickelalactones upon elimination of CO.